A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478600



Internal ID21136153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75807316..75870601hg38UCSC Ensembl
chr13:76381452..76444737hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3863286
hg1963286
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181874
Samples
Known GenesLMO7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478600
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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